Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs3892710 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 4
rs2395163 0.882 0.160 6 32420032 intergenic variant T/C snv 0.17 3
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 3
rs9275184 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs12660382
HCP5
0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs2395488
HCP5
0.882 0.160 6 31478132 non coding transcript exon variant A/G snv 0.34 3
rs2244839
HCP5 ; HCG26
0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs3916765
LOC102725019
0.882 0.200 6 32717773 upstream gene variant G/A snv 8.5E-02 3
rs3763309
TSBP1-AS1 ; BTNL2
0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 2
rs2246618
MICB
0.882 0.160 6 31511209 upstream gene variant C/T snv 0.32 2
rs2516424
MICB-DT
0.925 0.160 6 31480538 non coding transcript exon variant A/G snv 0.34 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 2
rs1980495
TSBP1-AS1
0.925 0.160 6 32379017 intron variant A/C snv 0.24 2
rs482759 1.000 0.080 6 32227240 upstream gene variant A/G;T snv 1
rs7454108 0.925 0.120 6 32713706 upstream gene variant T/C snv 9.1E-02 1